Senior Site Manager (Vivos)

Clinical Research Universe Featured Jobs

Posted: January 17, 2017

Job ID: 169

Job Summary

Term: Full-Time
Job Roles: Clinical Trial Monitoring
Required Education: Bachelor's degree or higher in a scientific or healthcare discipline preferred.
Required Experience: 4+ years

Job Description

Regional Site Managers (CRAs) support the goals of the Gen Med organization by initiating, monitoring, and closing out clinical study sites following GCP and ICH guidelines as well as SOPs and ensuring that study milestones are met. Central point of communication between investigational sites for all clinical trial related activities. Mentor to CRAs. Trial Lead CRA role when assigned. Performs additional roles and functions for US ICRO as assigned; such as participating/leading special project initiatives and committees. Is an essential contributor for the assessment and development of processes.

**These are REMOTE positions.

Understanding of medical and business knowledge relevant to clinical trial execution.
Minimum of seven years of CRA experience.
Solid understanding of clinical trial design, trial execution, and operations.
Trial Lead CRA experience.
Demonstrated ability to coordinate, organize, communicate, and manage trial site activities, with knowledge of when to escalate issues to management or clinical team.
Advanced understanding of clinical development, knowledge and experience in international (FDA, EMEA, ICH) and local regulations.
Excellent oral and written communication and presentation skills.
Ability to multi-task and prioritize multiple high-priority projects, site questions, CRA questions, and clinical team inquiries while managing responsibilities and deadlines.
Computer literacy and proficiency.
Experience as a CRA mentor.

If interested, please contact:

Anna Martinez
Vivos Professional Services